Genetic causes of hypomagnesemia, a clinical overview (Q33715342)

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Genetic causes of hypomagnesemia, a clinical overview (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27234911%20AND%20SRC:MED&resulttype=core&format=json

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renal tubular transport disease

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physiological absorption

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physiological phenomenon

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Daan H H M Viering

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Stephen B Walsh

series ordinal

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Detlef Bockenhauer

series ordinal

5

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publication date

27 May 2016

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1 July 2017

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page(s)

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issue

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Creative Commons Attribution 4.0 International

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copyright license

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on focus list of Wikimedia project

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copyright status

copyrighted

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exact match

https://scigraph.springernature.com/pub.10.1007/s00467-016-3416-3

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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TRPM6 forms the Mg2+ influx channel involved in intestinal and renal Mg2+ absorption

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

1 reference

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21 June 2018

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21 June 2018

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Hyperphenylalaninemia with high levels of 7-biopterin is associated with mutations in the PCBD gene encoding the bifunctional protein pterin-4a-carbinolamine dehydratase and transcriptional coactivator (DCoH).

21 June 2018

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21 June 2018

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21 June 2018

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Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

21 June 2018

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21 June 2018

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Kenny syndrome: evidence for idiopathic hypoparathyroidism in two patients and for abnormal parathyroid hormone in one.

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Maternal hypomagnesemia causes placental abnormalities and fetal and postnatal mortality.

21 June 2018

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EGF increases TRPM6 activity and surface expression

21 January 2018

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Association between activating mutations of calcium-sensing receptor and Bartter's syndrome

21 January 2018

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Altered renal distal tubule structure and renal Na(+) and Ca(2+) handling in a mouse model for Gitelman's syndrome.

21 January 2018

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Cardiac work up in primary renal hypokalaemia-hypomagnesaemia (Gitelman syndrome).

21 January 2018

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Cardiac arrhythmias due to severe hypokalemia in a patient with classic Bartter disease

21 January 2018

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SeSAME/EAST syndrome--phenotypic variability and delayed activity of the distal convoluted tubule.

21 January 2018

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Gitelman's syndrome revisited: an evaluation of symptoms and health-related quality of life.

21 January 2018

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Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia.

21 January 2018

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"Bartter-like" phenotype in Kearns-Sayre syndrome.

21 January 2018

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Nucleotide binding triggers a conformational change of the CBS module of the magnesium transporter CNNM2 from a twisted towards a flat structure

21 January 2018

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Fatal congenital myopathy and gastrointestinal pseudo-obstruction due to POLG1 mutations.

21 January 2018

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Molecular cloning and characterization of a novel gene family of four ancient conserved domain proteins (ACDP).

21 January 2018

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Mother-to-daughter transmission of Kenny-Caffey syndrome associated with the recurrent, dominant FAM111A mutation p.Arg569His

21 January 2018

1 reference

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Src-mediated inter-receptor cross-talk between the Na+/K+-ATPase and the epidermal growth factor receptor relays the signal from ouabain to mitogen-activated protein kinases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-016-3416-3

Distal convoluted tubule.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5440500

Recessive mutations in PCBD1 cause a new type of early-onset diabetes

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5440500

Chlorella and Spirulina: Green Supplements for Balancing the Body

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5440500

Evidence for parathyroid failure in magnesium deficiency

30 October 2018

1 reference

12 December 2020

A high prevalence of hypomagnesemia and hypermagnesemia in hospitalized patients

1 reference

12 December 2020

Oral versus intravenous magnesium supplementation in patients with magnesium deficiency

1 reference

12 December 2020

Micropuncture study of magnesium transport along the nephron in the young rat

1 reference

12 December 2020

Hypomagnesemic torsades de pointes

1 reference

12 December 2020

Bartter syndromes and other salt-losing tubulopathies

1 reference

12 December 2020

Neonates with Bartter syndrome have enormous fluid and sodium requirements

1 reference

12 December 2020

Frequency of hypomagnesemia and hypermagnesemia. Requested vs routine

1 reference

12 December 2020

Fractional excretion of magnesium in normal subjects and in patients with hypomagnesemia

1 reference

12 December 2020

10.1007/S00467-016-3416-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27234911%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

3 April 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27234911%20AND%20SRC:MED&resulttype=core&format=json

3 April 2020

1 reference